A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218066



Internal ID20785106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118023786..118024505hg38UCSC Ensembl
chr11:117894501..117895220hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586135
Supporting Variants
Samples
Known GenesTMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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